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²ÉÓÃÓͰ·ÓÍËáÊ®°ËÏ©»¹Ô­Pt(acac)2À´ÖƱ¸³öÔ¼2nm ptÄÉÃ×Á£×Ó£¬·ÖÉ¢¶ÈÒ²½ÏºÃ£¨ÏÂͼ1£©£¬µ«ÊÇÔڵõ½Á£×Ó½øÐÐIgepal-»·¼ºÍé-°±Ë®-TEOS°ü¸²µÄʱºò£¬³öÏֽϴóµÄÎÊÌâÎÞ·¨½øÐÐÕý³£°ü¸²
     °ü¸²±ÈÀý¿ªÊ¼²ÎÕÕÎÄÏ×Langmuir 2010, 26(21), 16469¨C16473
     Cyclohexane(25 mL) was mixed with igepal CO-630 (8.0 mL) and NH4OH solution (1.0 mL), and the mixture was stirred for 10 min. A NiPt particle dispersion in cyclohexane (25 mL, 10 mM with respect to the precursor concentration) was added into the mixture. After 30 s, TMOS (1.0 mL) was injected, and the resulting mixture was stirred for 60 min at room temperature. The NiPt@SiO2 particles were precipitated by adding methanol (10 mL) and were purified by a repetitive dispersion/precipitation cycle in ethanol.
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    In a 250 mL Erlenmeyer flask, 3 mL of Igepal CO-520 was added to 100 mL of cyclohexane, and the mixture wasstirred at room temperature for 5 min. Nine milligrams of Fe-Pt nanocrystals redispersed in 9 mL of cyclohexane was added to the stirring Igepal solution. After stirring for 5 min, 0.65 mL of 30% aqueous NH4OH solution was added dropwise to the mixture, followed by immediate addition of TEOS; 0.375-1.0 mL of TEOS was added, depending on the desired silica shell thickness, which could be increased from 3 to 13 nm by increasing the amount of TEOS. The mixture was stirred for 48 h, and then the SiO2-coated Fe-Pt nanocrystals were extracted from the cyclohexane phase by adding 50 mL of methanol. The cyclohexane phase was discarded. The nanoparticle dispersion was collected in a 100 mL, round-bottom flask and placed on a rotary evaporator to concentrate the dispersion down to a volume of 10 mL.
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